Basso, Manuela
University of Trento
2 papers on CoChatORCID 0000-0002-9278-8960
Most cited papers
- Verified
Spinocerebellar ataxia 38: structure–function analysis shows ELOVL5 G230V is proteotoxic, conformationally altered and a mutational hotspot
Ferrero, E., Di Gregorio, E., Ferrero, M., Ortolan, E., Moon, Y.-A., Di Campli, A., Pavinato, L., Mancini, C., Tripathy, D., Manes, M., et al. (2023) · Human Genetics
Genetic Neurodegenerative DiseasesHereditary Neurological Disorders
Cited by 9
- Verified
Spinocerebellar ataxia 38: structure-function analysis shows ELOVL5 G230V is proteotoxic, conformationally altered and a mutational hotspot
Ferrero, E., Gregorio, E. D., Ferrero, M., Ortolan, E., Moon, Y.-A., Campli, A. D., Pavinato, L., Mancini, C., Tripathy, D., Manes, M., et al. (2023) · Human Genetics
Genetic Neurodegenerative DiseasesHereditary Neurological Disorders
Cited by 9
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